chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
791759579175959TT57GENIChomozygous137934627
791762359176236TC63GENIChomozygous137999763
791768579176858CG57GENIChomozygous137999764
791768889176890TT56GENICpossibly homozygous137934628
791770469177047AG56GENIChomozygous137999765
791773649177376TGGGTGGATGGG37GENIChomozygous137934629
791783359178336CT57GENIChomozygous137999766
791797319179732CG45GENIChomozygous137999767
791797979179798G42GENIChomozygous137934630
791810889181089CT57GENICpossibly homozygous137999768
791811419181141TG46GENICpossibly homozygous137934631
791820909182091TC48GENIChomozygous137999769
791824869182487TG49GENIChomozygous137999770
791824879182488TA47GENIChomozygous137999771
791825909182590TCTTAT48GENIChomozygous137934632
791830549183055CT43GENIChomozygous137999772
791832759183276TC42GENIChomozygous137999773
791856659185666AT46GENIChomozygous137999774
791857819185782AG52GENIChomozygous137999775
791862349186235GA55GENIChomozygous137999776
791870709187071AG56GENIChomozygous137999777
791871589187159CT41GENIChomozygous137999778
791883399188340TG37GENICpossibly homozygous137999780
791886159188616AT48GENIChomozygous137999781
791892199189220GA69GENIChomozygous137999782
791893059189306T55GENIChomozygous137934633
791905599190560AG60GENIChomozygous137999783
791909459190946TC40GENIChomozygous137999784
791912679191268TA28GENIChomozygous137999785
791921299192129C11GENIChomozygous137934634
791925959192596TC42GENIChomozygous137999788
791934249193425AG54GENIChomozygous137999789
791939289193929TC43GENIChomozygous137999790
791942689194269T32GENICheterozygous403199519
791942199194220GA25GENICheterozygous154425179
791942689194269TC32GENIChomozygous154425180
791942199194220G25GENIChomozygous403199518
791840259184026GA1GENIChomozygous146827454
791840309184031AG1GENIChomozygous146827455